Abstract
Aim
The aim of this study is to assess the murine heart of normal embryos, neonates, and juveniles using high-frequency ultrasound.
Methods
Diastolic function was measured with E/A ratio (E wave velocity/A wave velocity) and isovolumetric relaxation time (IRT), systolic function with isovolumetric contraction time (ICT), percentage fractional shortening (FS %), percentage ejection fraction (EF %). Global cardiac performance was quantified using myocardial performance index (MPI).
Results
Isovolumetric relaxation time remained stable from E10.5 to 3 weeks. Systolic function (ICT) improved with gestation and remained stable from E18.5 onward. Myocardial performance index showed improvement in embryonic life (0.82–0.63) and then stabilized from 1 to 3 week (0.60–0.58). Percentage ejection fraction remained high during gestation (77%–69%) and then decreased from the neonate to juvenile (68%–51%).
Conclusion
The ultrasound biomicroscope allows for noninvasive in-depth assessment of cardiac function of embryos and pups. Detailed physiological and functional cardiac function readouts can be obtained, which is invaluable for comparison to mouse models of disease.
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References
Yu Q, Leatherbury L, Tian X, Lo CW. Cardiovascular assessment of fetal mice by in utero echocardiography. Ultrasound Med Biol. 2008;34(5):741–752.
Yu Q, Shen Y, Chatterjee B, Siegfried BH, et al. ENU induced mutations causing congenital cardiovascular anomalies. Development. 2004;131(24):6211–6223.
Lickert H, Takeuchi JK, Walls J, et al. Baf60c is essential for function of BAF chromatin remodeling complexes in heart development. Nature. 2004;432(7013):29.
Spurney CF, Lo CW, Leatherbury L. Fetal mouse imaging using echocardiography: a review of current technology. Echocardiography. 2006;23(10):891–899.
Phoon CK, Aristizabal O, Turnbull DH. 40 MHz Doppler characterization of umbilical and dorsal aortic blood flow in the early mouse embryo. Ultrasound Med Biol. 2000;26(8): 1275–1283.
Leatherbury L, Yu Q, Lo CW. Noninvasive phenotypic analysis of cardiovascular structure and function in fetal mice using ultrasound. Birth Defects Res C Embryo Today. 2003;69(1): 83–91.
Spurney CF, Leatherbury L, Lo CW. High-frequency ultrasound database profiling growth, development and cardiovascular function in C57BL/6J mouse fetuses. J Am Soc Echocardiogr. 2004;17(8):893–900.
Yu Q, Leatherbury L, Tian X, Lo CW. Cardiovascular assess¬ment of fetal mice by in utero echocardiography. Ultrasound Med Biol. 2007;34(5):741–752.
Hinton RB Jr, Alfrieri CM, Witt SA, et al. Mouse heart valve structure and function: echocardiographic and morphometric analyses from the fetus through the aged adult. Am J Physiol Heart Circ Physiol. 2008;294(6):480–488.
Zhou YQ, Foster FS, Parkes R, Adamson SL. Developmental changes in left and right ventricular diastolic filling patterns in mice. Am J Physiol Heart Circ Physiol. 2003;285(4): H1563–H1575.
Tiemann K, Weyer D, Djoufack PC, et al. Increasingmyocardial contraction and blood pressure in C57BL/6 mice during early postnatal development. Am J Physiol Heart Circ Physiol. 2003;284(2):H464–H474.
Teichholtz LE, Kreuler T, Herman MV, Gorlin R. Problems in echocardiographic volume determination:echocardio-graphic—angiographic correlations in the presence or absence of asynergy. Am J Cardiol. 1976;37(1):7–11.
Tei C, Ling L, Hodge DO, et al. New index of combined systolic and diastolic myocardial performance: a simple and reproductive measure of cardiac function—a study in normals and dialated cardiomyopathy. J Cardiol. 1995;26(6):357–366.
Bose AK, Mathewson JW, Anderson BE, et al. Initial experience with high frequency ultrasound for the newborn C57BL mouse. Echocardiography. 2007;24(4):412–419.
Srinivasan S, Baldwin Scott H, Aristizabal O, et al. Noninvasive, in utero imaging of mouse embryonic heart development with 40 Mhz echocardiography. Circulation. 1998;98(9): 912–918.
Russell N, Foley M, Kinsley B, Firth R, Coffey M, McAuliffe FM. Effect of pre-gestational diabetes on fetal cardiac function and structure. Am J Obstet Gynecol. 2008;199(3): 213–314.
Liu J, Du J, Zhang C, Walker JW, Huang X. Progressive troponin I loss impairs cardiac relaxation and causes heart failure in mice. Am J Physiol Heart Circ Physiol. 2007;293(2): H1273–H1281.
Zhou YQ, Zhu Y, Bishop J, et al. Abnormal cardiac inflow patterns during postnatal development in a mouse model of Holt-Oram syndrome. Am J Physiol Heart Circ Physiol. 2005; 289(3):H992–H1001.
Makikallio K, Jouppila P, Rasanen J. Human fetal cardiac function during the first trimester of pregnancy. Heart. 2005; 91(3):334–338.
Russell N, McAuliffe FM. First trimester fetal cardiac function. J Ultrasound Med. 2008;27(3):379–383.
Tsutsumi T, Ishii M, Eto G, Hota M, Kato H. Serial evaluation for myocardial performance in fetuses and neonates using a new Doppler index. Pediatr Int. 2002;41(6): 722–727.
Mu J, Qu D, Bartczak A, et al. Fgl2 deficiency causes neonatal death and cardiac dysfunction during embryonic and postnatal development in mice. Physiol Genomics. 2007;31(1):53–62.
Gui YH, Linask KK, Khowsathit P, Huhta JC. Doppler echocardiography of normal and abnormal embryonic mouse heart. Pediatr Res. 1996;40(4):633–642.
Kulandavelu S, Qu D, Sunn N, et al. Embryonic and neonatal phenotyping of genetically engineered mice. ILAR J. 2006; 47(2):103–117.
Stimpel T, Gershey EL. Selecting anesthetic agents for human safety and animal recovery surgery. FASEB J. 1991;5(7):2099–2104.
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Corrigan, N., Brazil, D.P. & McAuliffe, F.M. High-Frequency Ultrasound Assessment of the Murine Heart From Embryo Through to Juvenile. Reprod. Sci. 17, 147–157 (2010). https://doi.org/10.1177/1933719109348923
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DOI: https://doi.org/10.1177/1933719109348923